Alcon recalls 20 GA Totalplus Procedure Pak (Product #8065751079) due to possible inclusion of 25-gauge cannula instead of 20-gauge, which could cause incorrect surgical procedures.
There was a potential that a 25-gauge infusion cannula may be included within the procedure pak instead of a 20-gauge infusion cannula.
Alcon is recalling a specific surgical procedure kit that might contain a 25-gauge cannula instead of the required 20-gauge cannula. Using the wrong cannula size could lead to incorrect surgical procedures during eye surgery.
The procedure pak might include a 25-gauge infusion cannula instead of the required 20-gauge cannula. Using the wrong cannula size could lead to incorrect surgical procedures during eye surgery, potentially causing complications.
Surgical teams using the Alcon Constellation Vision System 20 GA Totalplus Combined Procedure Pak (Product #8065751079) for eye surgery are affected. Surgeons and their teams are most at risk.
Check for the product number 8065751079 on the label. The firm name on the label is Alcon Laboratories, Inc., Fort Worth, TX. The lot number is 2128524H.
Look for the product number 8065751079 and lot number 2128524H on the label.
The recall indicates a potential risk of using the wrong cannula size, but the product is not unsafe if the correct cannula is used. The manufacturer has not provided a fix.
The recall does not specify a remedy, so no action is required beyond checking the product label for the product number and lot number.
The recall does not mention a risk of serious injury, so this is considered a low-risk issue.
We’ve drafted a message you can send Alcon to request your refund or repair — edit it as you like.
Subject: Recall Z-1794-2020 — Alcon Alcon Hello, I own a Alcon that is covered by recall Z-1794-2020 from Alcon. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
